Crosslinking agents and flow control agents powdered coating compositions of carboxy containing copolymers epoxy

ABSTRACT

Powder coating compositions are disclosed. In general, individual powder coating compositions of this invention are a mixture of the following materials. A copolymer of an Alpha , Beta unsaturated carboxylic acid and an ethylenically unsaturated compound is formed in such proportions as to obtain a copolymer with a glass transition temperature in the range of 40*C to 90*C and a molecular weight (Mn) in the range of 2,500 to 8,500. The Alpha , Beta -unsaturated carboxylic acid is present in the copolymer from at least about 3 percent by weight to not more than about 10 percent by weight. Another material of the coating composition is an epoxy resin in the amount of 0.8 to 1.1 epoxy groups for each carboxy group in the copolymer. A third material utilized in forming the powder coating mixture is a flow control agent which forms at least 0.05 percent by weight of the mixture. The flow control agent is a polymer having a molecular weight (Mn) of at least 1,000. The flow control agent also has a glass transition temperature at least 50*C below the glass transition temperature of the copolymer.

ilnited States Patent Labana et al.

POWDERED COATING COMPOSITIONS OF CARBOXY CONTAINING COPOLYMERS, EPOXY CROSSLINKING AGENTS AND FLOW CONTROL AGENTS Inventors: Santokh S. Labana, Dearborn Heights; Amos Golovoy, Westland; Seymour Newman, Southfield, all of Mich.

Assignee: Ford Motor Company, Dearborn,

Mich.

Filed: Aug. 16, 1971 Appl. No.: 172,226

US. Cl. 260/836, 117/93.4 R, 117/126 GE, 117/126 GR, 117/132 BE, 260/37 EP, 260/41 R, 260/41 A, 260/41 B, 260/41 C, 260/830 R,

260/830 TW, 260/837, 260/DIG. 16

[51] Int. Cl C08g 45/04 [58] Field of Search 260/836, 837, 830 TW, 260/830 R [56] References Cited UNITED STATES PATENTS 3,305,601 2/1967 Hicks 260/836 3,409,592 11/1968 Landua.... 260/836 3,652,476 3/1972 Fellers 260/836 Primary Examiner-Paul Lieberman Attorney-Keith L. Zerschling and William E. Johnson [57] ABSTRACT Powder coating compositions are disclosed. In general, individual powder coating compositions of this invention are a mixture of the following materials. A copolymer of an a, B unsaturated carboxylic acid and an ethylenically unsaturated compound is formed in such proportions as to obtain a copolymer with a glass transition temperature in the range of 40C to 90C and a molecular weight (M,,) in the range of 2,500 to 8,500. The a, B-unsaturated carboxylic acid is present in the copolymer from at least about 3 percentby weight to not more than about 10 percent by weight. Another material of the coating composition is an epoxy resin in the amount of 0.8 to 1.1 epoxy groups for each carboxy group in the copolymer. A third material utilized in forming the powder coating mixture is a flow control agent which forms at least 0.05 percent by weight of the mixture. The flow control agent is a polymer having a molecular weight (M,,) of at least 1,000. The flow control agent also has a glass transition temperature at least 50C below the glass transition temperature of the copolymer.

4 Claims, No Drawings POWDERED COATING COMPOSITIONS OF CARBOXY CONTAINING COPOLYMERS, EPOXY CROSSLINKING AGENTS AND FLOW CONTROL AGENTS BACKGROUND OF THE INVENTION Powder coating compositions for use in the painting of surfaces are extremely desirable. Such coating compositions are desirable because they eliminate the solvents utilized in liquid paint systems as, for example, the paint system shown in U.S. Pat. No. 2,857,354, issued Oct. 21, 1958. A powder coating paint composition is curable by heat in a manner that little, if any, volatile material is given off to the surrounding environment. This, of course, is substantially different from a liquid paint system as the liquid paint vehicle must be volatilized during the drying of the'paint. Volatilization of the liquid vehicle carries such vaporized material into the surrounding ambient.

This invention is directed to powder coating compositions which are suitable for finishing surfaces of articles with a protective and decorative coating. The coatings produced by the compositions of this invention are comparable on all terms with the coating produced by the prior art liquid paint systems. The liquid paint system disclosed in U.S. Pat. No. 2,857,354 is apparently similar but, in reality, substantially different than the powder coating compositions of this invention. A full discussion of these differences is set forth in the last portion of this specification.

sitions and, more particularly, to powder coating com positions which are curable by heat. A powder coating composition formed in accordance with the teachings 'bis(4,5-epoxy-2-methyl The preferred ranges for individual contents of the materials for the powder coating compositions described above is as follows. The a,B unsaturated carboxylic acid which forms a portion of the copolymer in the mixture should be present in the copolymer in the range of at least 3 percent by weight to no more than 10 percent by weight. A desirable range of 01,3 unsaturated carboxylic acid in the copolymer is at least 4 percent by weight to nomore than 8 percent by weight with the most desirable copolymer containing approximately 5 percent by weight of the 01,6 unsaturated carboxylic acid. The desirable 01,3 unsaturated carboxylic acids are acrylic acid, methacrylic acid, maleic acid, itaconic acid and citraconic acid. Also, the preferred glass transition temperature for the copolymer is in the range of 50C to 80C with a molecular weight (FL) in the range of 3,000 to 6,500. The most desirable glass transition temperature for the copolymer is 60C to 70C with a molecular weight (,0 in the range of 3,000 to 4,000. With respect to the epoxy resins used in the powder coating mixture as the crosslinking agent, a number of bisphenol type epoxy resins, aliphatic diglycidyl ethers, diglycidyl esters and cycloaliphatic epoxy resins maybe used.'The desirable epoxy resins are diglycidyl ether of bisphenol A, diglycidyl ether of l,2-butanediol, cyclohexyl) adipate, solid epoxy resins obtained by reacting bisphenol A with diglycidyl ether of bisphenol A.

With respect to the flow control agents used in the powder coating mixture, an individual agent selected for a mixture may be an acrylic polymer having a glass of this invention comprises an intimate mixture of several materials. A first material of the mixture is a copolymer of an 0,5 unsaturated carboxylic acid and an ethylenically unsaturated compound in such proportions as to obtain a copolymer with a glass transition temperature in the range of 40C to 90C and with a molecular weight (m in the range of 2,500 to 8,500.

The carboxylic acid compound is present in the copoly-' mer from at least about 3 percent by weight to no more than about 10 percent'by weight. Another material of themixture is an'epoxy resin containing'two or more epoxy groups per molecule. The epoxyresin is present in the mixture in the amount of 0.8 to 1.1 epoxygroup's per each carboxy group in the copolymer. Another material of the mixture is a flowcontrol agent which forms control agent is a polymer having a molecular weight (fi of at least 1,000. The flow control agent also has a glass transition temperature at least C below the glass transition temperature of the copolymer.

ln greatee detail, the pow r coating composition formed in accordance with the teachings of this invention includes a small weight percent of acatalyst which produces a gel time for the powder coating composiat least 0.05 percent by weight of the'mixture. This flow transition temperature below the glass transition temperature of thevmixtures copolymer. Preferred acrylic polymers which may be used for the flow control agent arepolylauryl acrylate, polylauryl methacrylate, polybutyl acrylate, polybutyl methacrylate, poly( 2- ethylhexyl acrylate), poly(Z-ethylhexyl methacrylate) 40 and polyisodecyl methacrylate. a

The flow control agent may also be a fluorinated polymer having a surface tension, at the baking temperature of the powder, lower than that of the copolymer utilized .in the mixture. Preferred flow'control agents,

if the agent is a fluorinated polymer, are esters of polyethyleneglycol or polypropyleneglycol and fluorinated fatty acids. For example, an ester of polyethyleneglycol of molecular weight of over 2,500 and pertluoro octanoic'. acid is useful as aflow control polymer. In addition to the up unsaturated carboxylic acid monomer used in all copolymer-forming mixtures, other monomers which may be used are methyl methacrylate, butyl methacrylate, ethylmethacrylate, butyl 'acrylate, ethylacrylate, Z-ethylhexyl acrylate, styrene,

minutes. The preferred catalyst is one which produces a gel time of at least 1 minute but no greater than 10 minutes. In general, the catalyst is present in the range of from 0.05 percent by weight to 1 percent by weight of the weight of the mixture. The most desirable gel time produced by the catalyst is in a time range of from about 3 minutes to about l minutes. These catalyst gel times are at baking temperatures for the powder coating compositions in the range of 130C to 200C.

The powder coating compositions of thisinvention may also contain from about 6 percent by weight to about 35 percent by weight of a pigment. The various pigments already known in the art may be employed in the power coating compositions. The pigments are generally selected for color, appearance or corrosion protection properties.

A small weight percent of an antistatic agent may also be employed in the powder coating composition. For example, 0.05 percent by weight to 0.5 percent by weight of the powder coating composition may be an antistatic agent so that the coating may be applied in an electrostatic spraying operation.

DESCRIPTION OF THE PREFERRED EMBODIMENT A general discussion of the various materials which may be employed in the powder coating compositions of this invention will be set forth below. Also, a plurality of examples will be employed to show the manner in which various, individual, powder coating compositions, which fall within the scope of this invention, are prepared and utilized.

The principle material in individual powder coating compositions is a copolymer formed from an (1,,8 unsaturated carboxy acid such as acrylic acid and/or methacrylic acid and an ethylenically unsaturated monomer in such proportions as to obtain a copolymer with a glass transition temperature in the range of 40C to 90C and a molecular weight (fi in the range of 2,500 to 8,500. Other carboxylic acids such as maleic acid, itaconic acid, and citraconic acid are preferred monomers. The ethylenically unsaturated monomer employed to form the copolymer is any one, or a mixture of, the manydifferent monomers known to those skilled in the art. in forming the copolymer, the carboxylic acid monomer is present in the final copolymer from at least about 3 percent by weight to no more than about 10 percent by weight. The balance of the weight of the copolymer is formed from the ethylenically unsaturated monomers.

The preferred ethylenically unsaturated monomers which are employed to form the copolymer with the carboxylic acid monomer are methyl methacrylate, butyl methacrylate, butyl acrylate, ethyl acrylate, 2- ethylhexyl acrylate. Suitable modifying monomers such as styrene, alpha methyl styrene, acrylonitrile and methacrylonitrile can be used with the preferred monomers. When used, a modifying monomer is present in .the copolymer from a weight percent of about 0 percent by weight to no more than about 35 percent by weight. Thus, when the preferred ethylenically unsaturated monomers are used with the carboxylic acid monomer to form the copolymer, the acid monomer is present in the copolymer from 3 percent by weight to about 10 percent by weight, the modifying monomer is present from about 0 percent by weight to no more than about 35 percent by weight, and the preferred monomer is present from about 97 percent by weight to about 55 percent by weight.

The copolymers of the carboxylic acid monomers can be prepared by a variety of methods. Generally, a free radical initiator is needed to induce polymerization reaction. A large number of free radical initiatiors are known in the art. These include benzoyl peroxide, lauryl peroxide, t-butylhydroxyperoxide, acetylcyclohexane sulfonyl peroxide, diisobutyryl peroxide, di-( 2- ethylhexyl) peroxydicarbonate, diisopropyl peroxydicarbonate, t-butylperoxypivalate, decanoyl peroxide, azobis (Z-methylpropionitrile)etc. The polymerization is preferably carried out in solution using a solvent in which the copolymer is soluble. Toluene, xylene, dioxane, butanone, etc., ae suitable solvents for polymerization. If the carboxylic acid copolymer is prepared in solution, the solid copolymer can be obtained by evaporating the solvent under vacuum or spray drying techniques. Alternatively, the copolymer can be precipitated by pouring at a slow rate the solution into a nonsolvent liquid such as hexane, octane or water under a suitable agitation condition at a slow rate. The copolymer thus obtained should be further dried so that it contains less than three percent of the volatile liquids.

Carboxylic acid copolymers can also be prepared by emulsion polymerization, suspension polymerization, bulk polymerization of their suitable combinations. In these methods of preparing the copolymers, chain transfer agents may be required to control the molecu lar weight of the copolymer to a desired range.

For powder coating applications, molecular weight and molecular weight distribution of the (1,3 unsaturated carboxylic acid copolymer is importanLzCopolymer of average molecular weight (E71,) in the range of 2,500 to 8,500 are suitable. These copolymers, however, must not contain significant amount of higher molecular weight fractions. No more than 2 than of the copolymer can be of molecular weight greater than 20,000. The molecular weight distribution as measured by the ratio of weight aberage molecular weight to number average molecular weight (fig/M1,) should be in the range of 1.6 to 2.1. The preferred range of molecular weight distribution is in the range of 1.7 to 1.8.

Another one of the materials of individual ones of the powder coating compositions of this invention is an epoxy resin with two or more epoxy groups per molecule. Commercially available and other epoxy resins are described by H. Lee and K. Neville in Handbook of Epoxy Resins, published by McGraw Hill in 1957 at page 20, et seq. Of the resins described, solid epoxy resins of diglycidyl ether of the bisphenol type and epoxy novolac type materials are preferred. Liquid epoxy resins of the bisphenol diglycidyl ether type, aliphate epoxy resins and cycloaliphaticv epoxy resins, if used, must be employed in less than 12 parts for parts of the copolymer.

A flow control agent is also included in forming each individual ones of the powder coating compositions of this invention; The flow control agent forms at least 0.05 percent by weight of an individual powder coat ing. The flow control agent generally does not exceed about 4 percent by weight of any individualpowder coating composition. In general, the flow control agent is a polymer having a molecular weight (i of at least 1,000. Further, theflow control agent has a glass transition temperature at least 50C below'the glass transition temperature of the copolymer.

One type of material which is used as a flow control agent in the powder coating compositions is an acrylic polymer. Some acrylic polymers which are preferred as flow control agents are polylauryl acrylate, polylauryl methacrylate, polybutyl acrylate, polybutyl methacrylate, poly( Z-ethylhexyl acrylate) and poly(2-ethyhexyl methacrylate). Acylic polymers to be used as flow control agents can be prepared by polymerization of the acrylate or methacrylate monomers in bulk or in suitable solvent using well known free radical initiators. The amount of the initiator and the polymerization conditions are chosen so that polymer formed has molecular weighflfi above 1000. The preferred molecular weight range of the acrylate polymer/is above 5,000 The most preferred range of the acrylate polymer is 6,000 to 20,000.

Although polymeric acrylate flow control agents are preferred, fluorinated polymers have been found to act as flow control agents for the powder coating compositions. Such fluorinated polymers are esters of polyethyleneglycol or polypropyleneglycol and fluorinated fatty acids. Esters of polyethyleneglycol of molecular weight (R1,) of over 2500 and perfluoro oetanoic acid are useful as flow control agents for the compositions of this invention.

The powder coating compositions each contain a small, effective, weight percentage of a catalyst. in general, the catalyst is present in an individual composition in a range from 0.5 percent by weightt 1.0 percent by weight. The catalyst is selected to produce a gel time for the powder coating composition greater than at least 1 minute at the baking temperature of the composition. A suitable catalyst is also one which will produce a gell time that does not exceed 40 minutes. As used herein, the gell time of a coating composition is that time in which the coating composition develops elasticity and resistance to flow at the baking temperature.

Some catalysts which are suitable for use in the powder coating composition include tetralkylammonium salts, imidazole type catalysts, tertiary amines, triaryl phosphates and metal salts of organic carboxylic acids. The tetralkylammonium salts catalysts include the following: tetrabutyl ammonium chloride (bromide or iodide), tetraethyl ammonium chloride (bromide or iodide), tetramcthyl ammonium chloride, dodecyl dimethyl (2-phenoxyethyl) ammonium bromide and diethyl (2-hydroxy ethy) methyl ammonium bromide. Suitable catalysts of the imidazole type include: 2- methyl-4v-ethyl immidazole, imidazole, -methyl imidazole, imldazole,2- [(N-benzylanilino) methyl] -2- imidazoline phosphate, and 2-benzyl-2-imidazoline hydrochloride. Suitable tertiary amine catalyst for the powder coating compositions'of this invention include: tri-ethylene diamine, N,N-diethylcycohexylamirie,and N-methyl morpholine. The metal salts of organic carboxylic acid which are catalyst for the powder coatings of this inventioninclude but are not limitedto: stannous octoate, zinc naphthenate, cobalt naphthenate, zinc octoate, stannous 2-ethylhexoate, phenylmercurie pripionate, lead neodecanoate, dibutyl tin dilaurate and lithium benzoate. An example of triarylphosphate type catalystis triphenylphosphate,

The catalyst used in an individual powder coating composition is preferably solid atroom temperature and has a melting point of from 50C to 200C. As previously specified, the catalyst is present in a powder coating composition from 0.05 percent by weight to [.0 percent by weight of the total weight of, the powder composition. Further, the catalyst produces a gel time of at least 1 minute and no greater than 40 minutes. Generally, the preferred gel time of the composition is in the range of from 1 minute to approximately 10 minutes at the baking temperature of the composition.

, Since individual powder coating compositions of this invention can be applied to an artice to article painted by electrostatic methods, it is preferred to include a small weight percentage of an antistatic agent in such compositions so that the deposition thereof is accomplished in a proper manner. In particular, the antistatic agent is included in a range from 0.05 percent to L0 percent by weight of the total powder composition. SuiItable antistatic agents include, but are not limited to, tetralkylammonium salts as discussed previously and which also serve as catalysts. Other suitable antistatic agents include: alkyl-poly (ethylenoxy) phosphates as, for example, dibutyl-poly (ethyleneoxy) phosphate or alkylaryl poly (ethyleneoxy) phosphates as, for example, ethyl benzyl poly (ethyleneoxy) phosphate.

- In order to give individual powder coating compositions of this invention a suitable color, a pigment is ineluded in the coating composition. In general, the pig ment forms from about 6 percent by weight to about 35 percent by weight of the total powder coating composition. Pigments which are suitable for powder coating compositions include, but are not limited to, the following: basic lead silico chromate percent by weight (orange); titanium dioxide 30 percent by weight (white); titanium dioxide 15 percent by weight plus ultra marine blue lO percent by weight (blue); phthalocyanine blue 7v percent by weight plus titanium dioxide 10 percent by weight (green); ferrite yellow 7 percent by weight plus titanium dioxide 10 percent by weight (yellow); carbon black pigment 6 percent by weight (black); black iron oxide 10 percent by weight (black);

chromium green oxide 8 percent by'weight plus titanium dioxide 10 percent by weight (green); quindo red 5 percent by weight plus titanium dioxide 16 percent by weight (red); and iron oxide transparent orange pigment 10 percent by weight (orange).

Having generally described the various materials I which are employed in formulating the powder coating compositions of this invention, a plurality of examples will beset forth to illustrate various individual powder coating compositions. Y

' EXAMPLE I The monomers, methacrylic acid 5 percent by weight, methyl methacrylate percent by weight and butyl methacr ylate 45 percent by weight, are mixed together. Three weight percent of a catalyst 2,2"-azobis- 7 fraction of heat supplied from an external heater. After 'the'addition of the monomer mixture is complete, the

refluxing is maintained by external heat source for 3 additional hours. v v

The solution is poured into shallow stainlesssteel trays. These trays are placed in a vacuum oven and the solvent evaporated therefrom. As the solvent is removed, the copolymer solution becomes more concentrated. The temperature of the vacuum oven is raised to about 110C. Drying is continued until the solvent content of the copolymer is below 3 percent. The trays are cooled and the copolymer collected and ground to pass through 20 mesh screen. The copolymer has a glass transition temperature of 53C and a molecular weight m of 4,000.

One hundred parts by weight of the ground copolymer are mixed with the following materials:

Epon 1001 (See page 4-66 of Handbook 26 parts of Epoxy Resins Tetrabutyl ammoniu m bromide 0.2 parts Polylauryl acrylate(M,,=l0,000) 0.5 parts Titanium dioxide 30 parts The materials are mixed together in a ball mill for 2 hours. The mixture is milled rolled at 85C to 90C for 5 minutes. The solid obtained is ground in a ball mill to pass through a 140 mesh screen.

The resulting powder thus obtained is a powder coating composition of the invention. The powder is sprayed on an electrically grounded, steel panel by using electrostatic powder spray gun operating at 50 KV charging voltage. After spraying, the panel is heated at 175C for 20 minutes.

The coating obtained on the panel has good adhesion to the steel panel and good impact strength. The coating also is applied to and has good adhesion on panels of glass, brass, zinc, aluminum, copper and bronze. The coating obtained is not soluble in toluene, gasoline, butanone or methanol.

EXAMPLE 2 The procedure of Example 1 is repeated. The formation of the copolymer, however, begins with a monomer mixture having methacrylic acid 8 percent by weight, methyl methacrylate 52 percent by weight and butyl methacrylate 40 percent by weight. Three weight percent of the catalyst AlBN is employed. When the procedure of Example 1 is followed, the resulting copolymer has a glass transition temperature of 58C and a molecular weight of 4,000.

One hundred parts of the copolymer produced is mixed with the same additional ingredients set forth in Example 1, except using 50 parts of Epon 1001. The quality of the painted panels obtained after application of the powder coating to various materials is about the same as achieved in Example 1.

EXAMPLE 3 A monomer mixture having the following composi tion is prepared: acrylic acid 3 percent by weight, methyl methacrylate 48 percent by weight, and butyl methacrylate 49 percent by weight. The monomer mixture is processed in the same manner as described in Example 1 with 3 percent by weight of the catalyst AlBN employed. The resulting copolymer has a glass transition temperature of 56C and a molecular weight of 4,000. One hundred parts of the copolymer produced is mixed with the same additional ingredients described in Example 1, except 21.0 parts of Epon 1002 (See page 4-66 of Handbook ofEpoxy Resins) are used.

The powder coating composition obtained by following the process steps set forth in Example 1 is applied to test panels in the same manner as described in Example 1. The coating is baked at a temperature of 170C for 30 minutes. The coating obtained has good adhesion to steel, glass, brass, zinc, aluminum, copper and bronze.

EXAMPLE 4 Epon 828 (See page 4-66 of Handbook 10 parts of Epoxy Resins) Tetrabutylammonium chloride 0.1 part Polybutylacrylate (fi.=9000) 4 parts Titanium dioxide 15 parts Ultra marine blue 10 parts The above ingredients are mixed together and processed in accordance with the procedure of Example 1 to obtain a powder coating composition. The powder coating composition is sprayed on various test panels of steel, glass, brass, zinc, aluminum, copper and bronze. The coating obtained on each test panel after curing of the powder coating composition at a temperature of 200C for 10 minutes is of good quality, and is solvent and scratch resistant.

EXAMPLE 5.

A monomer mixture having the following composition is prepared: methacrylic acid 3 percent by weight, methyl methacrylate 50 percent by weight and butyl methacrylate 47 percent by WeighL The monomers are reacted as described in Example 1 to produce a copolymer. In this case, 6 percent by weight of the catalyst AlBN is employed. The resulting copolymer has a glass transition temperature of 53C and a molecular weight of 2,000.

One hundred parts by weight of the copolymer obtained is mixed with the following materials;

Epon 828. 6.5 parts 2-methyl'4-ethylimidazole 0.05 parts Dibu'tyl poly(ethyleneoxy) phosphate 0.05 parts Polyisdodecylrnethacrylate 4-parts Titanium dioxide 10 parts Phthalocyanine blue 7 parts A powder coating composition is obtained byfollowing' the process steps set forth in Example 1. The coating composition is applied to a series of test panels and baked at the temperature of and for the same time as Example 4. The coating obtained on the various test panels is of good quality with resect to its adhesion appearance and impact characteristics.

EXAMPLE 6 Amonomer A monomer having the following composition is prepared: methacrylic acid 6 percent 1 by weight, butyl methacrylate .29 percent by weight and methyl methacrylate 65 percent by weight. ,The monomer is reacted as set forth in Example 1 in order to produce a copolymer. Four percent by weight of the catalyst AlBN is employed in reacting .thermonomer mixture to form the copolymer. The copolymer has a glass transition temperature of 65C and a molecular weight of 3,000.

One hundred parts by weight of the copolymer obtained is added to the following materials:

l,4-butanediglycidyl ether 10 parts Triethylene diamine 01 part Tetraethylammonium chloride 0.05 parts Polylaurylmethacrylate(M 6000) 2 pans Phthaloycanine green 7 parts Titanium dioxide 10 parts The above described materials are processed as described in Example 1 in order to produce a powder coating composition. The powder coating composition is applied to test panels as described in Example I and baked on the panels at a temperature of 150C for minutes.

The coating obtained has good adhesion to steel,

glass, brass, zinc, aluminum, copper and bronze and isinsoluble in toluene, gasoline, methanol and butanone.

EXAMPLE 7 EXAMPLE 9 A monomer mixture having the following composition is formed: methacrylic acid 7 percent by weight, methyl methacrylate 38 percent by weight, isobutyl acrylate 25 percent by weight, alpha methyl styrene l5 percent by weight and methacrylonitrile 15 percent by weight. The monomer mixture is reacted in the same manner as described in Example 1. Three percent of the catalyst AIBN is employed. The resulting copolymer has a glass transition temperature of 46C and a molecular weight of 4,500.

One hundred parts of the ground copolymer obtained is added to the following materials.

Epon 1002 60 parts Dodecyldimethyl (Z-pigenoxy-ethyl ammonium bromide (M,.=3400) 0.5 parts Polyethylene glycol perfluoro octonoate 2 parts Black iron oxide 10 parts E on 1004 (See page 4-66 of Handbook 11.0 parts 0 Epoxy Resin: Tetramethylammonium chloride lpart Poly(2 eth lhexyl acrylate) 2 parts Ferrite yel ow 7 parts Titanium dioxide 10 parts This mixture is processed as described in Example 1 in order to form a powder coating composition. The powder coating composition is applied to test panels as described in Example 1. The panels are baked at a temperature of 180C for 5 minutes. The adhesion quality of the powder coating after baking on the various test panels is good. The coating on each panel possesses good solvent and scratch resistance.

EXAMPLE 8 A monomer mixture having the following composition is formed: acrylic acid 8 percent by weight, ethyl acrylate 30 percent by weight, methyl methacrylate 40 percent by weight, vinyl chloride 22 percent by weight.

The monomer mixture is polymerized byusing 2'weight percent by the catalyst AlBN as the initiator.

One hundred parts of the ground copolymer obtained is added to the following materials:

Epon I002 70 parts Tri'methyl benzyl ammonium chloride 0.1 part Poly(2-ethylhexyl acrylate) (M51 L000) 2 parts Carbon black 6 parts The above materials are mixed and processed as set forth in Example 1. The resulting powder coating composition is applied to test panels as specified in Example l. The coating composition is baked at 170C for 15 minutes. All the painted panels exhibit good adhesion and solvent resistance properties.

The mixture so formed is processed as described in Example 1 to produce a powder coating composition. This powder coating composition is applied to test panels as it is described in Example 1. The coated panels are baked at C for 15 minutes. The coating on each panel has good adhesion and solvent resistance.

EXAMPLE 10 A monomer mixture having the following composition is prepared: methacrylic acid 2 percent by weight, methyl methacrylate 55 percent by weight, and butyl methacrylate 43 percent by weight. The monomer mixture is reacted as described in Example 1 with 6 per cent by weight of the catalyst AlBN. The resulting copolymer has afglass transition temperature of 55C and a molecular weight of 3,000.

One hundred parts by weight of the ground copolymer is mixed with the following materials:

Epon i002 l5 parts .Tetraethylammonium' bromide 1 part Ethyl benzyl (ethyleneoxy) phosphate 0.5 parts Poly (2-ethylhexyl acrylate) 0.4 parts Chromium green oxide 8 parts '10 parts Titanium dioxide The above mixture is processed asdescribed in Example l to produce a powder coating composition. The powder coating composition is applied to a plurality of test panels. .Thepanels are baked at a temperature of C for 20 minutes. The adhesion to the test panels of the powder coating materialis poor and coating has a tendency to chip and crack.

" EXAMPLE 1i i A monomer m'ixture'is formed having the following compositionzitaconic acid 3 percent by weight, methyl methacrylate 50 percent by weight, 2-ethylhexyl acry-' late l7 percent by weight and acrylonitrile 28 percent by weight. The monomer mixture is processed as set forth in Example 1 in order to forma copolymer. Four percent by weight of the catalyst AIBNis added. The copolymer formed has a glass transition temperature of 60C and a molecular weight of 4,000.

' l. One hundred parts by weight of the ground copoly mer is mixed with the following materials:

24.0 parts 0.5 parts 0.05 parts is applied Polyethylene glycol Epon i002 Stannous octoste Tetraethylsmmonium bromide perfluoro octonoate 2 parts Quindo red 5 parts for dioxide parts is good The mixture above described is processed as set forth in Example 1 to produce a powder coating composition. The powder coating composition isapplied to test panels as described in Example 1. The panels are baked at 150C fr minutes. The adhesion to the panels of the powder coating isgood and the coating possesses good solvent resistance.

EXAMPLE 12 A monomer mixture having the following composition is prepared: maleic acid 4 percent by weight, nhexyl methacrylate 38 percent by weight, butyl methacrylate percent by weight and acrylonitrile 33 percent by weight. A copolymer is formed from this monomer mixture in accordance with the same procedure as is outlined in Example 1. In this case, 1.5 percent by weight of the catalyst AIBN is added. The copolymer produced has a glass transition temperature of 40C and a molecular weight of 7,500.

The ground copolymer (100 parts by weight) is added to the following materials:

bis(2-methyl-4,5-epoxycyclohexy) adipate 10 parts zinc octoate 0.8 part Tetrabutylammonium iodide 1.0 parts Polybutyl acrylate 2.0 parts Iron oxide transparent orange 10 parts The above ingredients are mixed together and processed in accordance with the procedure of Example 1 to obtain a powder coating composition. The powder coating composition is sprayed on various test panels of steel, glass, brass, zinc, aluminum, copper and bronze. The coating obtained on each test panel after curing of the powder coating composition at a temperature of 140C for 20 minutes is of good quality, and is solvent and scratch resistant.

EXAMPLE 13 bis(2-methyl-4,5-epoxycyclohexyl)adipate 10 parts Tetrabutylammonium bromide 2 parts Poly(2-ethylhexyl acrylate) 3.5 parts Carbon black 6 parts The above ingredients are mixed together and processed in accordance with the procedure of Example 1 to obtain a powder coating composition. The powder coating composition is sprayed on various test panels. The coating obtained on each test panel after curing of the powder coating composition at a temperature of 160C for 10 minutes is of good quality. Also, the coating obtained on each test panel is insoluble in toluene, gasoline, methanol and butanone.

EXAMPLE 14 A monomer mixture having the following composition is prepared: acrylic acid 4 percent by weight, methyl methacrylate 52 percent by weight and isobutyl methacrylate 44 percent by weight. A copolymer is formed from this monomer mixture in accordance with the same procedure as is outlined in Example 1. In this case, 5 percent by weight of the catalyst AIBN is added. The copolymer produced has a glass transition temperature of C and a molecular weight of 3,200.

The ground copolymer parts by weight) is added to the following materials 1,2-butane diglycidyl ether 7.5 parts Tetrabutylammonium bromide 2 parts Polylauryl acrylate 4 parts Titanium dioxide 30 parts The above ingredients are mixed together and processed in accordance with the procedure of Example 1 to obtain a powder coating composition. The powder coating composition is sprayed on various test panels of steel, brass, glass, zinc, aluminum, copper and bronze. The coating obtained on each test panel after curing of the powder coating composition at a temperature of C for 10 minutes is of good quality and is solvent and scratch resistant.

EXAMPLE 15 A monomer mixture having the following composition is prepared: methacrylic acid 5 percent by weight, methyl methacrylate 67 percent by weight, ad n-butyl methacrylate 28 percent by weight. A copolymer is formed from this monomer mixture in accordance with the procedure as is outlined in Example 1. In this case 4 percent by weight of the catalyst AIBN is added. The copolymer produced has a glass transition temperature of 73C and a molecular weight of 3,000.

The ground copolymer (100 parts by weight) is added to the following materials:

Epon 828 11 parts Tetrabutylammonium chloride 0.7 part Polybutyl acrylate 2 parts Titanium dioxide 30 parts The above ingredients are mixed together and processed in accordance with the procedure of Example 1 toobtain a powder coating composition. The powder coating composition is sprayed on various testpanels. The coating obtained on each test panel after curing of the powder coating composition at. a temperature of C for 15 minutes is of good quality. Also, each of the test panel coatings is resistant to and insoluble 'in toluene, gasoline, methanol and butanone.

EXAMPLE 1s A monomer mixture having the following composition is prepared: acrylic acid 5 percent by weight, methyl methacrylate 32 percent by weight, ethyl acrylate 25 percent by weight, isobutyl acrylate 8 percent by weight and styrene 30 percent by weight. A copolymer is formed from this monomer mixture in accordance with the same procedure as is outlined in Example 1. In this case, 3 percent by weight of the catalyst AIBN is added. I

The ground copolymer (100 parts by weight) is added to the following materials:

13 Epon 1001 40 parts Tetraethylamrnonium bromide 1 part Polyisodecyl methacrylate(M,,-=5000) l.5 parts Titanium dioxide 30 parts The above ingredients are mixed together and processed in accordance with the procedure of Example I to obtain a powder coating composition. The powder coating composition is sprayed on various test panels of steel, glass, brass, zinc, aluminum, copper and bronze.

The coatings obtained on each test panel after curing of the powder coating composition at a temperature of 140C for minutes is of good quality and has good adhesion characteristics. The powder coating composition on each panel is resistant to the solvents previously mentioned.

EXAMPLE l7 A monomer mixture having the following composition is prepared: methacrylic acid 6 percent by weight, methyl methacrylate 49 percent by weight, 2- ethylhexyl acrylate 15 percent by weight, alpha methyl styrene percent by weight and acrylonitrile 10 percent by weight. A copolymer is formed from this monomer mixture using 4 percent by weight of the catalyst AlBN.

The ground copolymer (100 parts by weight)is added to the following materials:

Epon [002 50 parts Tetraethylammonium bromide 0.4 part Poly(2-ethylhexyl acrylate) 2 parts Titanium dioxide parts The above ingredients are mixed together and processed in accordance with the procedure of Example I to obtain a powder coating composition. The powder coating composition is sprayed on various test panels of steel, glass, brass, zinc, auminum, copper and bronze. The coating obtained on each test'panel after curing of the powder coating composition at a temperature of 170C for 20 minutes is of good quality and resistant to the aforementioned solvents.

EXAMPLE 18 A monomer mixture having the following composition is prepared: acrylic acid 6 percent by weight, butyl acrylate percentlby weight, methyl methacrylate 24 percent by weight and styrene 30 percent by weight. A copolymer is formed from this monomer mixture in accordance with the same procedure as in outlined in Example 1. In this case, 4 percent by weight of the catalyst AlBN is added. The copolymer produced has a glass lCfor 10 minutes is of good quality and is resistant to the aforementioned solvents.

EXAMPLE 19 A monomer mixture having the following composition is prepared: methacrylic acid 7 percent by weight, butyl methacrylate 23 percent by weight, ethyl acrylate 15 percent by weight, methyl methacrylate 30 percent by weight and styrene25 by weight. A copolymer is formed from this monomer mixture in accordance with the same procedure as in outlined in Example 1. In this case, 4 percent by weight of the catalyst AlBN is added.

The ground copolymer parts by weight) is added to the following materials:

Epon 1004 80 pans Tetraethylammonium bromide l.0 parts Polylauryl acrylate 0.5 part Titanium dioxide 30 parts The above ingredients are mixed together and processed in accordance with the procedure of Example 1 to obtain a powder coating composition. The powder coating composition is sprayed on various test panels of steel, glass, brass, zinc, aluminum, copper and bronze. The coating obtained on each test panel after curing of the powder coating composition at a temperature of C for 30 minutes is of good quality and resistant to the aforementioned solvents.

EXAMPLE 20 Epon l004v 90 parts Tetraethylammonium' bromide 0.5 part Polylauryl acrylate 2.5 parts 30 parts transition temperature of 40C and a molecular weight 5 The ground copolymer 100 parts by weight) is added to the following materials:

Epon 1002 50 parts Tetraethylammonium bromide 0.5, part Polylauryl acrylate 10 parts Titanium dioxide 30 parts The above ingredients are mixed together and processed in accordance withthe procedureof Example 1 to obtain a powder coating composition. The powder coating composition is sprayed on various test panels of steel, glass, brass, zinc, aluminum, copper and bronze. The coating obtained on each test panel after curing of the powder coating composition at a temperature of Titanium dioxide The'above ingredients are mixed together and pro- I cessed in accordance with the procedure of Example 1 to obtain a powder coating composition. The powder coating composition'is sprayed on various test panels of steel, glass; brass, zinc, aluminum, copper and bronze. The coating obtained on each testpanel after curing of the powder coating composition at a temperature of C for 30 minutes is of good quality. Also the coatings are resistant to and insoluble in toluene, gasoline, methanol and butanone.

The use of glycidyl methacrylate copolymers and discarboxylic acid cross linking agents in a liquid paint system is described in U.S. Pat. No. 2,857,354. However, the powder coating compositions of this invention are substantially different than the liquid paint compositions described in the examples of that patent. This difference can be best illustrated by attempting to prepare powder coating compositions by evaporating the solvents from the liquid paint systems described in the examples of the patent. Dry powders cannot be prepared from the compositions of Examples 4 and 5 of the patent. Powders prepared from the compositions of Examples l, 2, 3 and 6, when deposited on a metal panel, do not fuse together to form a film when the panels are baked at 150 to 200C for minutes. The baked coatings on test panels are not smooth, but rather, are rough. Also the baked coatings possess very low gloss, and have a lack of flexibility and adhesion. It, therefore, can be concluded that compositions which are generally suitable for liquid paint systems are not necessarily suitable for powder paints by simply evaporating the solvents therefrom.

The use of dicarboxylic acid as a cross linking agent for glycidyl methacrylate terpolymers is mentioned in US. Pat. No. 3,058,947. In order to test these materials, compositions of Example VII of this patent are dried by evaporating solvents under vacuum. The materials are ground to pass through a 200 mesh screen. Samples of the ground powder are depoisted on metal panels and baked at 160C for 45 minutes. The coatings obtained show an abundance of craters, are inferior in gloss and smoothness, and lack the impact properties described in the Example Vll. It is, therefore, concluded that there is a substantial difference in paint films produced on a panel when the coating is produced on one hand by a liquid system, and, on the other hand, by a powder system. Other improvements specific to the powders are needed in order to obtain paints of acceptable quality. The reason for the difference between the properties and'appearance of powder coatings derived by solvent evaporation from a liquid coating and the liquid coating itself are not clear. It is, however, certain that the powders obtained by drying liquid paint compositions are not useful for powde coating compositions.

There has been disclosed herein powder coating compositions which may be employed in the painting of articles. Many modifications of this invention will be apparent to those skilled in the art in view of this secification. It is intended that all such modifications which fall within the scope of this invention be included within the appended claims.

What we claim is:

1. A powder coating composition, which exclusive of pigment and antistatic agent comprises:-(A) a copolymer of an a, B unsaturated carboxylic acid and an ethylenically unsaturated compound in such proportions,

that said copolymer has a glass transition temperature ir the range of 40C to C and a molecular weight (M,,) in the range of 2,500 to 8,500, said unsaturated carboxylic acid being present in said copolymer from at least about 3 percent by weight to no more than about l0 percent by weight;

B. a cross linking agent formed from an epoxy resin having two or more epoxy groups per molecule, said epoxy resin being present in said powdercoating composition in an amount from 0.8 to L1 epoxy groups per each carboxy groupof-saidcopolymer to achieve substantialcross linking of said copolymer; and (C) a flow control'agent present from at least 0.05 percent to about 4.0 percent by weight of the mixture, said flow control agent being a polymer having a molecular weight (Kl of at least 1,000 and a glass transition temperature at vleast 50C below the glass transition temperature of said copolymer, said flow control agent further being a polymer or a copolymerselected from the group consisting of acrylate esters, methacrylate esters and polyethylene or polypropylene glycol esters of fluorinated fatty acids.

2. The powder coating composition of claim 1 wherein: said acrylic ester is selected from the group consisting of polylauryl acrylate, polylauryl methacrylate, polybutyl acrylate, polybutyl methacrylate, poly (Z-ethylhexylacrylate) and poly (Z-ethylhexyl methac-' rylate).

3. The powder coating composition of claim 1 wherein said a, B unsaturated acid is selected from the group consisting of acrylic acid, methacrylic acid, ma-; 

2. The powder coating composition of claim 1 wherein: said acrylic ester is selected from the group consisting of polylauryl acrylate, polylauryl methacrylate, polybutyl acrylate, polybutyl methacrylate, poly (2-ethylhexyl acrylate) and poly (2-ethylhexyl methacrylate).
 3. The powder coating composition of claim 1 wherein said Alpha , Beta unsaturated acid is selected from the group consisting of acrylic acid, methacrylic acid, maleic acid, itaconic acid, and citraconic acid.
 4. The powder coating composition of claim 1 wherein: said epoxy cross linking agent is selected from the group consisting of: bisphenol type epoxy resins, aliphatic diglycidyl ethers, diglycidyl esters, and cycloaliphatic epoxy resins. 